News
SBNS 2025 Briefing Part 1 - Redura® in the UK —Ten Years Key Insights
2025.09.29

1.Meeting Information 

On 26 September 2025, Day 3 of SBNS 2025 at Ashton Gate Stadium, Bristol, the 08:30 industry breakfast sponsored by Severn Healthcare focused on Medprin Dural Patches the UK experience. 


The session was chaired by Nigel Mendoza and Sam Hattige. Two speakers shared UK data and experience: Kevin ONeil (Imperial College Healthcare NHS Trust & Cleveland Clinic London) presented 10 YearsExperience with ReDura,followed by William Singleton (Bristol Royal Hospital for Children & UHBW) on paediatric duroplasty (reported separately).



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2.Redura Experience shared by Kevin ONeil 

A. Position & overall appraisal 

  • Repair philosophy: restore the anatomical barrierleaving the dura unrepaired may increase risks of CSF leak, impaired healing, and infection in specific scenarios.

  • Material rationale: autografts are limited; allo/xenografts raise ethical/immunologic/pathogen concerns; non-resorbable synthetics carry foreign-body issues; thus resorbable synthetics best approximate an idealsubstitute.


B. Redura® material & handling 

  • Engineering & material: electrospun PLA non-woven; slightly elastic, hydrophobic, aiding watertight closure and suturable handling.

  • OR behaviour: resists tearing, trims/holds sutures well under tension/CSF gradient; low adhesion to brain favours safe re-entry.

  • Biologic course: host dural ingrowth with resorption; routine experience suggests low inflammation/infection signal.


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C. Indications & scenarios 

  • Large dural defects (tumour, infection/attenuation, trauma/prior surgery);

  • Dural augmentation or high CSF gradient (e.g., posterior fossa, periventricular);

  • Intradural spinal closures;

  • Watertight-critical contexts (e.g., ventriculostomy, with brachytherapy/chemowafers) and revision cases needing non-adhesive, re-entry-friendly patches.


D. Representative cases (as shown) 

(1)Massive cranial defect in revision (patient from Sudan)

  • Persistent large dural gap; tried other product to overlay, attempts tended to sink.

  • First use of Redura® cut-to-fit achieved stable barrier;

  • operative takeaway: choose overlay vs underlay strategically by location/forces.


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(2)Dura-involved tumour

  • Thickened enhancing dura with a pinhole and blood ingress risk.

  • Sutured + overlay to block ingress; good closure achieved. 


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(3)Temporal tumour extending into the temporal horn (valve effect)

  • Dynamic CSF gradient and tissue stretch.

  • Surgeons comment: Redura®s elasticity & suturability feel as good asor better thanautograft for a controlled watertight repair. 


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(4)Re-entry experience

  • On recent returns to the field, the patch showed low adherence to brain, aiding clean plane dissection. 

E.Evidence and follow-up

A prospective RCT demonstrated non-inferiority to a synthetic comparator with very low CSF-leak rates; the principal limitation was 6-month follow-up, yet no device-on-brain safety signal emerged. Animal data indicate 12-week dural-cell replacement/integration.

F.Practical checklist

  • Closure strategy: suture-secure, watertight first; add sealant as reinforcement, not as a replacement for sutures.

  • Prioritise for: posterior fossa/periventricular, large defects, intradural spine, and revision surgery needing strength + low adhesion.

  • Pathway & QA: standardise sizing/suture/sealant; track CSF leak/infection/re-op/LOS for continuous quality assurance.

G.Bottom line

A resorbable, suturable, hydrophobic, low-adhesion patch with ten years of UK use, ReDura® is well-suited to high-risk watertight closures and fits a suture-first, sealant-as-adjunctphilosophy.


Next (Part II): William Singleton on paediatric duroplastychild-specific anatomy/physiology, closure tactics, and CSF-related complication prevention.